Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP53568.RAR0mSK5xa7P4P7dvxsYHfCFPGkHv5G86E8b3FgfdnfjY130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP53568.RAR0mSK5xa7P4P7dvxsYHfCFPGkHv5G86E8b3FgfdnfjY130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP53568.RAR0mSK5xa7P4P7dvxsYHfCFPGkHv5G86E8b3FgfdnfjY130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP53568.RAR0mSK5xa7P4P7dvxsYHfCFPGkHv5G86E8b3FgfdnfjY130_provenance.
- NP53568.RAR0mSK5xa7P4P7dvxsYHfCFPGkHv5G86E8b3FgfdnfjY130_assertion description "[We evaluated the influence of common genetic variation in the NER pathway on bladder cancer risk by analyzing 22 single nucleotide polymorphisms (SNP) in seven NER genes (XPC, RAD23B, ERCC1, ERCC2, ERCC4, ERCC5, and ERCC6).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP53568.RAR0mSK5xa7P4P7dvxsYHfCFPGkHv5G86E8b3FgfdnfjY130_provenance.
- NP53568.RAR0mSK5xa7P4P7dvxsYHfCFPGkHv5G86E8b3FgfdnfjY130_assertion evidence source_evidence_literature NP53568.RAR0mSK5xa7P4P7dvxsYHfCFPGkHv5G86E8b3FgfdnfjY130_provenance.
- NP53568.RAR0mSK5xa7P4P7dvxsYHfCFPGkHv5G86E8b3FgfdnfjY130_assertion SIO_000772 16537713 NP53568.RAR0mSK5xa7P4P7dvxsYHfCFPGkHv5G86E8b3FgfdnfjY130_provenance.
- NP53568.RAR0mSK5xa7P4P7dvxsYHfCFPGkHv5G86E8b3FgfdnfjY130_assertion wasDerivedFrom gad-20150221 NP53568.RAR0mSK5xa7P4P7dvxsYHfCFPGkHv5G86E8b3FgfdnfjY130_provenance.
- NP53568.RAR0mSK5xa7P4P7dvxsYHfCFPGkHv5G86E8b3FgfdnfjY130_assertion wasGeneratedBy ECO_0000203 NP53568.RAR0mSK5xa7P4P7dvxsYHfCFPGkHv5G86E8b3FgfdnfjY130_provenance.
- gad-20150221 importedOn "2015-02-21" NP53568.RAR0mSK5xa7P4P7dvxsYHfCFPGkHv5G86E8b3FgfdnfjY130_provenance.